A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932430



Internal ID22707728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102559163..102573211hg38UCSC Ensembl
chr14:103025500..103039548hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3814049
hg1914049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382138
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932430
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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